Huddart 2002.
| Methods | randomized controlled trial, not placebo‐controlled | |
| Participants | n = 95, lung, gynecological, genitourinary, other cancer; concomitant treatment: chemotherapy | |
| Interventions | drug = Epoetin alpha dose = 10000 IU sc TIW hb‐target = 12‐14 g/dL planned ESA duration = during chemotherapy |
|
| Outcomes | Hb response, reticulocyte, survival, QoL, safety | |
| Notes | study number = 88443 | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Adequate sequence generation? | Unclear risk | no description |
| Allocation concealment? | Unclear risk | no description |